Trends in contact lens microbial keratitis 1999 to 2015: a retrospective clinical review.


Journal

Clinical & experimental ophthalmology
ISSN: 1442-9071
Titre abrégé: Clin Exp Ophthalmol
Pays: Australia
ID NLM: 100896531

Informations de publication

Date de publication:
08 2019
Historique:
received: 08 08 2018
revised: 18 01 2019
accepted: 10 02 2019
pubmed: 26 2 2019
medline: 29 8 2020
entrez: 26 2 2019
Statut: ppublish

Résumé

Contact lens microbial keratitis (CLMK) is the most common cause of microbial keratitis in our community. Define the trend in rate of CLMK and define patient demographics/culture results that may have a predictive value in patients with CLMK. Retrospective review of clinical records of patients with MK. All patients with positive corneal scraping between 1999 and 2015 at the Princess Alexandra Hospital, Brisbane, Queensland identified through local microbiology database. Trend in CLMK tested with chi-squared test of peak 3 years vs other years and Poisson regression of interrupted time series. Patient characteristics predictive of CLMK were defined by creating a polynomial regression model by stepwise variable selection. Yearly rate of CLMK. Records of 895 episodes of MK were included. The most common: risk factor was contact lens wear (324, 36.2%), isolated organism was Pseudomonas aeruginosa (P. aeruginosa 181, 55.9%) and treatment was monotherapy with a fluoroquinolone 172, 53%). CLMK was most common between 2009 and 2011 (49.5% vs other years 32%, P < 0.001). Poisson regression of the interrupted time series showed there was a significant decrease in the rate over time after 2010 (P < 0.001). Independent factors predictive of CLMK in multivariate regression were young age (15-49 years) and corneal culture positive for P. aeruginosa CONCLUSIONS AND RELEVANCE: The rate of CLMK in our community ranged between 32% and 50% and the rate of disease appears to have peaked during 2009 to 2011 and subsequently declined.

Sections du résumé

IMPORTANCE
Contact lens microbial keratitis (CLMK) is the most common cause of microbial keratitis in our community.
BACKGROUND
Define the trend in rate of CLMK and define patient demographics/culture results that may have a predictive value in patients with CLMK.
DESIGN
Retrospective review of clinical records of patients with MK.
PARTICIPANTS
All patients with positive corneal scraping between 1999 and 2015 at the Princess Alexandra Hospital, Brisbane, Queensland identified through local microbiology database.
METHODS
Trend in CLMK tested with chi-squared test of peak 3 years vs other years and Poisson regression of interrupted time series. Patient characteristics predictive of CLMK were defined by creating a polynomial regression model by stepwise variable selection.
MAIN OUTCOME MEASURES
Yearly rate of CLMK.
RESULTS
Records of 895 episodes of MK were included. The most common: risk factor was contact lens wear (324, 36.2%), isolated organism was Pseudomonas aeruginosa (P. aeruginosa 181, 55.9%) and treatment was monotherapy with a fluoroquinolone 172, 53%). CLMK was most common between 2009 and 2011 (49.5% vs other years 32%, P < 0.001). Poisson regression of the interrupted time series showed there was a significant decrease in the rate over time after 2010 (P < 0.001). Independent factors predictive of CLMK in multivariate regression were young age (15-49 years) and corneal culture positive for P. aeruginosa CONCLUSIONS AND RELEVANCE: The rate of CLMK in our community ranged between 32% and 50% and the rate of disease appears to have peaked during 2009 to 2011 and subsequently declined.

Identifiants

pubmed: 30801907
doi: 10.1111/ceo.13484
doi:

Substances chimiques

Anti-Bacterial Agents 0
Fluoroquinolones 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

726-732

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2019 Royal Australian and New Zealand College of Ophthalmologists.

Auteurs

Matthew Green (M)

Ophthalmology department, Gold Coast University Hospital, Southport, Queensland, Australia.
School of Optometry and Vision Science, University of New South Wales, Sydney, New South Wales, Australia.

Sergio Sara (S)

Ophthalmology department, Sydney Eye Hospital, Sydney, New South Wales, Australia.

Ian Hughes (I)

Ophthalmology department, Gold Coast University Hospital, Southport, Queensland, Australia.

Andrew Apel (A)

Ophthalmology department, Princess Alexandra Hospital, Brisbane, Queensland, Australia.

Fiona Stapleton (F)

School of Optometry and Vision Science, University of New South Wales, Sydney, New South Wales, Australia.

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